StellarCaps capsule quality documents and product records
Quality Documents

StellarCaps Quality Document Center

Quality records, applicable product registrations, and technical documents for empty capsule procurement review

Quality documents buyers may request

This page is a procurement document entry for empty capsule buyers. Before sampling or bulk orders, buyers can ask StellarCaps to confirm which records are applicable to the selected capsule material, capsule size, target market, packaging requirement, and batch plan.

COA and specification sheet for the selected capsule type
Batch and traceability records for procurement review
Sample records and packaging information before trial filling
Market-specific document review based on buyer requirements

What China CDE status A means

For China pharmaceutical projects, CDE registration status A is a regulatory signal for the listed capsule excipient. It means the listed item is recorded by China's CDE as approved for use in marketed drug products. It is not a universal quality certificate, so buyers should review the current official record together with COA, specifications, batch records, registered product name, and project-specific requirements.

Quality Management Systems

Quality Management System Information
Empty Hard Gelatin Capsules — Registration No. F20240000553, China CDE status A
Empty HPMC / Hypromellose Capsules — Registration No. F20240000554, China CDE status A
GMP-aligned Production Practices

Market-Specific Documentation

Market-specific dietary documents available when applicable
Customer documentation requests reviewed case by case

Technical Documents

COA - Certificate of Analysis
TDS - Technical Data Sheet
MSDS - Material Safety Data Sheet
Third-party Test Reports Available on Request

Market Compliance Support

BSE/TSE Statement Available When Required
Country-specific Documentation Support